159 related articles for article (PubMed ID: 16155418)
1. Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.
Tsien F; Morava E; Talarski A; Marble M
Clin Dysmorphol; 2005 Oct; 14(4):177-181. PubMed ID: 16155418
[TBL] [Abstract][Full Text] [Related]
2. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.
Piram A; Ortolan D; Peres LC; Pina-Neto JM; Riegel M; Schinzel A
Am J Med Genet A; 2003 Jul; 120A(2):247-52. PubMed ID: 12833408
[TBL] [Abstract][Full Text] [Related]
3. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
[TBL] [Abstract][Full Text] [Related]
4. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
Tatar A; Oztas S; Yakut T; Ors R
Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
[TBL] [Abstract][Full Text] [Related]
5. A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities.
Huang S; Xia Y; Ding H; Wang Y; Wu Y; Chen S; Zhuang J; Li P
Fetal Pediatr Pathol; 2021 Jun; 40(3):256-261. PubMed ID: 31805817
[TBL] [Abstract][Full Text] [Related]
6. Complex chromosome re-arrangement 45,X,t(Y;9) in a girl with sex reversal and mental retardation.
de Ravel TJ; Fryns JP; Van Driessche J; Vermeesch JR
Am J Med Genet A; 2004 Jan; 124A(3):259-62. PubMed ID: 14708098
[TBL] [Abstract][Full Text] [Related]
7. Case report: Y;6 translocation with deletion of 6p.
Klein OD; Backstrand K; Cotter PD; Marco E; Sherr E; Slavotinek A
Clin Dysmorphol; 2005 Apr; 14(2):93-96. PubMed ID: 15770132
[TBL] [Abstract][Full Text] [Related]
8. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
[TBL] [Abstract][Full Text] [Related]
9. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
[TBL] [Abstract][Full Text] [Related]
10. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
11. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born.
Fernández-Novoa MC; Vargas MT; Granell MR; Carreto P
Prenat Diagn; 2004 Jun; 24(6):414-7. PubMed ID: 15229838
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 1(q42-->qter): a new case with a mild phenotype.
Concolino D; Cinti R; Ferraro L; Moricca MT; Strisciuglio P
J Med Genet; 1998 Jan; 35(1):75-7. PubMed ID: 9475102
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 16p: a longitudinal profile and photo essay.
Sommer A; Pastore M; Wenger G
Am J Med Genet A; 2006 Jan; 140(2):174-9. PubMed ID: 16353251
[TBL] [Abstract][Full Text] [Related]
16. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.
Abuelo DN; Ahsanuddin AN; Mark HF
Am J Med Genet; 2000 Oct; 94(5):392-9. PubMed ID: 11050625
[TBL] [Abstract][Full Text] [Related]
17. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
18. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
19. Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1).
Hiraki Y; Fujita H; Yamamori S; Ohashi H; Eguchi M; Harada N; Mizuguchi T; Matsumoto N
Am J Med Genet A; 2006 Aug; 140(16):1773-7. PubMed ID: 16835918
[TBL] [Abstract][Full Text] [Related]
20. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
Petković I; Barisić I; Bastić M; Hećimović S; Bago R
Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
